PlainRecalls
FDA Devices Moderate Class II Terminated

Pilling Aortic Punch, 4.0 mm Standard Tip, REF 353440

Reported: February 26, 2020 Initiated: January 13, 2020 #Z-1269-2020

Product Description

Pilling Aortic Punch, 4.0 mm Standard Tip, REF 353440

Reason for Recall

There is a potential for the device packaging to become compromised; thus, the sterility of the device cannot be guaranteed.

Details

Recalling Firm
TELEFLEX MEDICAL INC
Units Affected
1764 units
Distribution
Worldwide
Location
Morrisville, NC

Frequently Asked Questions

What product was recalled?
Pilling Aortic Punch, 4.0 mm Standard Tip, REF 353440. Recalled by TELEFLEX MEDICAL INC. Units affected: 1764 units.
Why was this product recalled?
There is a potential for the device packaging to become compromised; thus, the sterility of the device cannot be guaranteed.
Which agency issued this recall?
This recall was issued by the FDA Devices on February 26, 2020. Severity: Moderate. Recall number: Z-1269-2020.